Canonical Allele Identifier: CA2629506473
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720815_74720872del , CM000677.2:g.74720815_74720872del GRCh38
NC_000015.9:g.75013156_75013213del , CM000677.1:g.75013156_75013213del GRCh37
NC_000015.8:g.72800209_72800266del NCBI36
NG_008431.1:g.3274_3331del
NG_008431.2:g.3274_3331del
NG_061374.1:g.9659_9716del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1254-96_1254-39del MANE Select ENSP00000369050.3:n.1254-96_1254-39del
ENST00000379727.7:c.1254-96_1254-39del ENSP00000369050.3:n.1254-96_1254-39del
ENST00000395048.6:c.1254-96_1254-39del ENSP00000378488.2:n.1254-96_1254-39del
ENST00000395049.8:c.1167-96_1167-39del ENSP00000378489.4:n.1167-96_1167-39del
ENST00000562201.5:c.*491-96_*491-39del ENSP00000455340.1:n.*491-96_*491-39del
ENST00000564596.5:c.*93_*150del ENSP00000457668.1:n.*93_*150del
ENST00000566503.1:c.471-96_471-39del ENSP00000455846.1:n.471-96_471-39del
ENST00000567032.5:c.1254-96_1254-39del ENSP00000456585.1:n.1254-96_1254-39del
ENST00000569630.5:c.*843-96_*843-39del ENSP00000455051.1:n.*843-96_*843-39del
ENST00000612821.4:c.1170-96_1170-39del ENSP00000479744.1:n.1170-96_1170-39del
ENST00000617691.4:c.1167-96_1167-39del ENSP00000482863.1:n.1167-96_1167-39del
NM_000499.3:c.1254-96_1254-39del NP_000490.1:n.1254-96_1254-39del
XM_005254185.1:c.1254-96_1254-39del XP_005254242.1:n.1254-96_1254-39del
NM_000499.5:c.1254-96_1254-39del NP_000490.1:n.1254-96_1254-39del
NM_001319216.2:c.1167-96_1167-39del NP_001306145.1:n.1167-96_1167-39del
NM_001319217.2:c.1254-96_1254-39del MANE Select NP_001306146.1:n.1254-96_1254-39del